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(11) | EP 0 061 689 A1 |
| (12) | EUROPEAN PATENT APPLICATION |
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| (54) | Radiation sensitive polymer materials |
| (57) A radiation sensitive polymer material comprising a polymer having (a) one ore more
repeating units of the formula:
wherein R is an alkyl group, a halogen atom, a hydrogen atom or a dimethylamino group, and (b) an addition polymerizable repeating unit derived from a compound having a CH2 = C group in the molecule, and if necessary, one hydrate of metal chloride or nitrate, can give a positive type resist having excellent resistance to dry etching and being highly sensitive to radiation. |
BACKGROUND OF THE INVENTION
i) Field of the invention
[0001] The present invention relates to radiation sensitive polymer materials, particularly positive type radiation sensitive polymer materials having high radiation sensitivity.
ii) Description of the prior art
[0002] In recent years, there is a tendency to require integrated circuits (IC) having higher density and higher integration. In the manufacture of IC, the formation of fine resist patterns having line width of less than 1 pm is thus required.
[0003] Radiation sensitive resists sensitive to radiations such as electron beams, X-rays and ion beams are suitable for the formation of fine resist patterns.
[0005] Radiation sensitive resists of negative type can, considering their reaction mechanism, inherently withstand influences caused by dry etching which is conducted at the time of fine pattern formation, and are good in sensitivity but poor in resolution.
[0006] On the other hand, radiation sensitive resists of positive type are inherently better in resolution than the negative type, considering the reaction mechanism. However, these positive type resists are attacked at their end portions in dry etching operation, and poorer in sensitivity than the negative type resists.
SUMMARY OF THE INVENTION
[0007] An object of this invention is to provide a radiation sensitive polymer material for positive type resists overcoming disadvantages of the porior art wherein the resolution of it is as good as that of conventional positive type radiation sensitive resists and the sensitivity and resistance to attack in dry etching operation are improved close to respective levels of conventional negative type radiation sensitive resists.
[0008] The above object can be achieved by the use of polymers having aromatic rings. When these polymers are subjected to irradiation of radiations such as electron beam, X-rays and ion beam, their molecular chains are cut effectively and thereby sensitivity improves. Also, they become less susceptible to attack in dry etching. The sensitivity is further improved when the polymers having aromatic rings possess substituents at the para-position. The sensitivity can be improved much further when the polymers having aromatic rings are used together with hydrates of metal chlorides or hydrates of metal nitrates.
[0009] The present invention provides the following radiation sensitive polymer materials [I] or [II]. Polymer material [I]
[0010] A radiation sensitive polymer having
(a) 10 to 100% by mole of one or more repeating units of the formula:
wherein R is a hydrogen atom, a lower alkyl group preferably having 1 to 6 carbon
atoms, a lower alkoxy group preferably having 1 to 6 carbon atoms, a halogen atom,
or a dialkylamino group, and
(b) 90 to 0% by mole of an addition polymerizable repeating unit derived from a compound
having
group in the molecule. Polymer material [II]
[0011] A radiation sensitive polymer material comprising:
a polymer having .
(a) 10 to 100% by mole of one or more repeating units of the formula (1) mentioned above, and
(b) 90 to 0% by mole of an addition polymerizable repeating unit derived from a compound
having
group in the molecule, in an amount of 80 to 99.9% by weight, preferably 90 to 99.9%
by weight, and
(c) at least one compound selected from hydrates of metal chlorides and metal nitrates in an amount of 20 to 0.1% by weight, preferably 10 to 0.1% by weight.
BRIEF DESCRIPTION OF THE DRAWING
[0012] The attached drawing is a graph showing a relationship between the electron beam quantity irradiated to a positive type radiation sensitive polymer material according to the present invention and its film thickness after development.
DESCRIPTION OF PREFERRED EMBODIMENTS
[0013] In the above polymer material [I] or [II], when there is present in the polymer the addition polymerizable repeating unit derived from a compound having
group in an amount more than 90% by mole, the sensitivity of the polymer to radiation such as electron beam, X-rays, ion beam, etc., becomes low and the resistance to dry etching is lowered remarkably.
[0014] When, in the above polymer material [II], there is present the hydrate of metal chloride or metal nitrate, the component (c), in an amount less than 0.1% by weight, the polymer material [II] does not show the adding effect of the component (c) on improved sensitivity to radiations such as electron beam, X-rays and ion beam. When the amount of the hydrate exceeds-20% by weight, the sensitivity of the material [II] to radiations worsens.
[0015] The polymer having (a) one or more repeating units of the formula (1) and (b) the addition polymerizable repeating unit is explained in detail below.
[0016] In the formula (I), the lower alkyl group includes methyl, ethyl, propyl, and the like, the lower alkoxy group includes methoxy, ethoxy, propoxy, and the like, the halogen atom includes chlorine, bromine, iodine, and the like, and the dialkylamino group wherein the dialkyl moiety preferably having 2 to 6 carbon atoms includes dimethylamino, diethylamino, and the like.
[0017] Preferable examples of the repeating units represented by the formula (1) include the followings:
etc.
[0018] These repeating units.may be present in the polymer as the component (a) singly or in combination of two or more of them.
[0019] The addition polymerizable repeating unit (b) can be represented by the formula:
wherein R1 is a lower alkyl group preferably having 1 to 3 carbon atoms or a phenyl group; R2 is -COOR3 (in which R3 is Cl-6 alkyl or phenyl), -COOH, -CN, -COR4 (in which R4 is C1-6 alkyl),
or a lower alkyl group preferably having 1 to 6 carbon atoms. The repeating unit of the formula (2) can be derived from a compound having
group in the molecule.
[0020] Preferable examples of the compounds each having
group in the molecule which can give an addition polymerizable repeating unit are alkyl esters of methacrylic acid such as methyl methacrylate, ethyl methacrylate, propyl methacrylate,-isopropyl methacrylate, butyl methacrylate, isobutyl methacrylate, t-butyl methacrylate, cyclohexyl methacrylate, etc.; methacrylic acid; methacrylonitrile; ketones such as methyl isopropenyl ketone; styrene derivatives such as a-methylstyrene; isobutylene; phenyl methacrylate, etc. Among these compounds, methacrylic acid, methyl methacrylate, methacrylonitrile and methyl isopropenyl ketone are more preferable. Each of these compounds can be used singly.
[0021] Preferable examples of the polymer having the repeating units of the formulas (1) and (2) are as follows:
(molecular weight (M.W.) 50,000)
(MW 80,000, copolymerization ratio (CPR) 0.5/0.5)
(MW 30,000, CPR 0.5/0.5)
(MW 50,000, CPR 0.5/0.5)
(MW 10,000, CPR 0.8/0.2)
(MW 80,000, CPR 0.1/0.9)
(MW 30,000, CPR 0.5/0.5)
(MW 10,000, CPR 0.8/0.2)
(MW 70,000, CPR 0.3/0.7)
(MW 100,000, CPR 0.2/0.8)
(MW 150,000, CPR 0.12/0.88)
[0022] The polymer having the repeating units of the formulas (1) and (2) itself has good sensitivity to radiation, and when a predetermined amount of the component (c) is added to the polymer, the sensitivity to radiation is further improved effectively.
[0023] Examples of the metal chloride hydrates, the component (c) include AlCl3·6H2O, CaCl2·6H2O, COCl2·6H2O, FeCl3·6H2O, CuCl2·2H2O, NiCl2·2H2O, PbCl2·2H2O, MnCl2·4H2O, CrCl3·6H2O· Examples of the metal nitrate hydrates include Al(NO3)3·9H2O, ZN(NO3)2·6H2O, In(NO3)3·3H2O, Ca(NO3)2· 4H20, Cr(N3)3·9H2O, CO(NO3)2·O6H2O,Fe(NO3)3.9H2/,Cu(NO3)2· 3H20, Ni(NO3)3·6H2O, Mn(N03)2.6H20. Among these hydrates, preferable ones are metal chloride hydrates of CoCl2·6H2O, FeCl3·6H2O, CuCl2·2H2O, NiCl2·2H2O, MnCl2·4H2O and CrCl3·6H2O as well as metal nitrate hydrates of Al(N03)3. 9H20, Zn(NO3)2·6H2O ,IN(NO3)3·3H2O, Cr(NO3)2·9H2O, Co(NO3)2·6H2O, Fe(NO3)3·9H2O, Ni(NO3).6H2O and Mn(NO3)2· 6H20. Each of these compounds is used singly.
[0024] The polymer material [I] or [II] is used as a positive type resist material by dissolving it in a conventional organic solvent such as toluene, methyl isobutyl ketone or N-methylpyrrolidone and the like.
[0025] Solubility of the polymer material [II] in the above organic solvent can be improved by adding such an organic acid as maleic acid, citraconic acid or the like thereto.
[0026] Hereinunder, the present invention is further explained in detail referring to Examples. Raw materials used for preparing organic polymers having the repeating unit represented by the formula (1) were synthesized as follows.
Synthesis Example 1
[0027] There were mixed 13.4 g of propiophenone, 4.5 g of paraformaldehyde, 12.2 g of piperidine hydrochloride, 0.25 cc of concentrated hydrochloric acid and 50 cc of ethanol. The mixture was refluxed for about 1 hour, and after addition of another 4.5 g of paraformaldehyde, the whole mixture was further refluxed for about 2 hours. This mixture was subjected to recrystallization from an acetone-ethanol solution to obtain phenyl β-piperidino isopropyl ketone hydrochloride (white, needle-like crystals).
[0028] Next, 10 g of this salt was heated at 200°C for 3 hours in 50 ml of N-methylpyrrolidone. After cooling and washing, phenyl isopropenyl ketone was obtained by distillation under reduced pressure (b.p.: 35 to 50°C/1 mmHg).
Synthesis Example 2
[0029] In a 1-liter three-necked flask were placed 92 g of toluene, 300 ml of carbon disulfide and 147 g of anhydrous aluminum chloride powder. To this, was added dropwise slowly in about 1 hour 130 g of propionic anhydride with mechanical stirring. The resulting mixture was refluxed for 3 hours until there was no generation of HC1 gas. After having been allowed to cool, the above reaction solution was transferred into 500 ml of an ice- water cooling medium, and the organic solvent layer in the solution was extracted with ether.
[0030] Next, this ether layer was water-washed, dried by an ordinary method to remove the water and distilled under reduced pressure to obtain p-methylpropiophenone (b.p.: 85 to 90°C/4 mmHg).
[0031] Next, there were mixed 14.8 g of p-methylpropiophenone, 4.5 g of paraformaldehyde, 12.2 g of piperidine hydrochloride, 0.25 ml of concentrated hydrochloric acid and 50 ml of absolute ethanol. The mixture was refluxed for about 1 hour and, after further addition of 3.0 g of paraformaldehyde, the whole mixture was refluxed for about 3 hours. After cooling, the above reaction solution was subjected to recrystallization from an acetone-ethanol solution in the same manner as described in Synthesis Example 1, to obtain white, needle-like crystals of a-piperidinomethyl-p-methylpropiophenone hydrochloride. Subsequently, 26.8 g of the above salt and 12.3 g of potassium t-butoxide were refluxed for about 5 hours in 100 ml of t-butanol.
[0032] Next, to the above reaction solution was added 200 ml of water. The mixture was extracted with ether and the extract was dried over a desiccating agent and subjected to distillation under reduced pressure to obtain p-methylphenyl isopropenyl ketone (b.p.: 70 to 80oC/1 to 2 mmHg).
Synthesis Example 3
[0033] In a 1-liter three-necked flask were placed 108 g of anisole, 300 ml of carbon disulfide and 147 g of anhydrous aluminum chloride powder. To this, was added dropwise slowly in about 1 hour 130 g of propionic anhydride with mechanical stirring. The whole mixture was refluxed for 5 hours until there was no generation of HC1 gas. After having been allowed to cool, the above reaction solution was subjected to the same procedure as described in Synthesis Example 2 to obtain p-methoxy- propiophenone (b.p.: 115 to 118°C/4 mmHg).
[0034] Next, there were mixed 16.4 g of p-methoxy- propiophenone, 4.5 g of paraformaldehyde, 12.2 g of piperidine hydrochloride, 0.25 ml of concentrated hydrochloric acid and 50 ml of absolute ethanol. This mixture was refluxed for about 1 hour and, after further addition of 3.0 g of paraformaldehyde, the whole mixture was refluxed for about 5 hours. Subsequently, this reaction solution was subjected to recrystallization from an acetone-ethanol solution in the same manner as described in Synthesis Example 2, to obtain white, needle-like crystals of a-piperidinomethyl-p-methoxypropiophenone hydrochloride.
[0035] Subsequently, 28.4 g of the above salt and 12.3 g of potassium-t-butoxide were refluxed for about 4 hours in 100 ml of t-butanol. After having been allowed to cool, this mixture was distilled under reduced pressure in the same manner as described in Synthesis Example 1 to give p-methoxyphenyl isopropenyl ketone (b.p.: 113 to 115°C/2 mmHg).
Synthesis Example 4
[0036] p-Chlorophenyl isopropenyl ketone, p-bromophenyl isopropenyl ketone and p-iodophenyl isopropenyl ketone were synthesized by using the same procedures as described in Synthesis Examples 1 to 3. Namely, firstly p-halogenated propiophenone was synthesized by the Friedel-Crafts reaction by using propionyl chloride instead of propionic anhydride. Subsequently, by the Mannish reaction was obtained white crystals of a-piperidinomethyl-p-halogenated propiophenone hydrochloride. Lastly, by a deamination reaction was obtained p-halogenated phenyl isopropenyl ketone.
Example 1
[0037] Using 0.1 g of azobisisobutyronitrile as a polymerization initiator, 10 g of phenyl isopropenyl ketone obtained in Synthesis Example 1 was statically polymerized at 80°C for 10 hours in a sealed tube containing nitrogen gas.
[0038] The polymer obtained was dissolved in about 10 ml of methyl isobutyl ketone. The solution obtained was transferred into about 500 ml of methanol to give a white precipitate of the above polymer. The weight average molecular weight of the polymer measured by liquid chromatography was about 50,000 in terms of that of polystyrene.
[0039] The polymer obtained was dissolved in methyl isobutyl ketone to obtain a resist solution wherein the solid polymer content was 15% by weight. Subsequently, this solution was spin-coated on a silicon wafer at 2000 rpm to form a polymer film of 0.8 pm thick.
[0040] The wafer obtained was prebaked at 150°C for 30 minutes and then transferred to an electron beam irradiation apparatus wherein an electron beam having an acceleration voltage of 15 kV was applied to the prebaked wafer in vacuum so as to give different dosages to different portions. Then, the wafer was taken out from the apparatus and dipped for 2 minutes in a developer consisting of methyl isobutyl ketone and isopropyl alcohol (35:65 by volume) for development. The wafer developed was rinsed with isopropyl alcohol to dissolve the irradiated portions. Thicknesses of the polymer film which had different thickness in portions depending upon different dosages were measured by the use of a Talystep (a thin film level difference meter, mfd. by Taylor Hobson Ltd., U.K.). Film thicknesses of retained portions after development (normalized) were plotted against irradiation amounts (exposure dose) of the electron beam (coulomb/cm2), by which a curve showing sensitivity to electron beam as shown in the attached drawing was obtained. The minimum exposure dose giving zero film thickness was obtained from the drawing to be 6 x 10-6 coulomb/cm2. Thus, the polymer of the present invention had a sensitivity 10 times or more as high as that of, for example, poly(methyl methacrylate).
[0041] Subsequently, the wafer was subjected to ion etching under an argon gas pressure of 2.0 x 10 4 Torr and ion energy density of 0.25 w/cm2. The polymer of the present invention showed an ion etching speed of 150 R/min compared to 200 Å/min in the case of a silicon oxide film. This indicates that ething of the substrate becomes possible by coating resist film of the present polymer having a thickness of at least two times that of the silicon oxide film, considering non-uniformity of etching and the like.
Example 2
[0042] Using 0.1 g of azobisisobutyronitrile as a polymerization initiator, 8 g of p-chlorophenyl isopropenyl ketone obtained in Synthesis Example 4 and 5 g of methyl methacrylate were statically polymerized at 80°C for 6 hours in a sealed tube containing enclosed nitrogen gas. The copolymer obtained was refined in the same manner as described in Example 1 to obtain a white precipitate. Measurement by liquid chromatography revealed that the copolymer had a weight average molecular weight of about 80,000 in terms of that of polystyrene. Also, measurement of NMR spectrum for this copolymer dissolved in an acetone-d6 solution revealed that the copolymer contained 50% by mole of p-chlorophenyl isopropenyl ketone.
[0043] The copolymer was dissolved in methyl isobutyl ketone to obtain a resist solution containing 15% by weight of the copolymer. In the same manner as described in Example 1, a polymer film of 1.0 pm thick was formed on a silicon wafer at 2000 rpm by the spin coating method.
[0044] The silicon wafer was prebaked at 1500C for 30 minutes. Then, the prebaked wafer was kept in a sample room maintained at 10-3 Torr and was subjected to irradiation of soft X-rays having a wavelength of 5.4 R supplied from a molybdenum anticathode of rotational water cooling type (acceleration voltage: 10 kV, 500 mA) with varying exposure doses.
[0045] The wafer irradiated was dipped in a developer consisting of methyl isobutyl ketone and isopropyl alcohol (35 : 65 by volume) for 2 minutes for development. Then, the wafer was rinsed with isopropyl alcohol to dissolve the irradiated portions.
[0046] In the same manner as described in Example 1, retained film thicknesses after development (normalized) were plotted against exposure dose. From the curve obtained, the minimum exposure dose giving zero film thickness was found to be 30 mJ/cm2Ú This fact indicates that the above resist had high sensitivity as a positive type resist. Also, ion etching was applied under argon gas in the same manner as in Example 1. This polymer gave an ion etching speed of 170 Å/min which showed the excellency of the polymer in ion etching resistance.
Example 3
[0047] Using the same procedures as described in Examples 1 and 2, polymers of various compositions (polymer Nos. 1 to 9 in Tabre 1) were obtained by radical polymerization at 80°C for 10 hours using as a polymerization initiator azobisisobutyronitrile. The polymers were refined in the same manner as described in Example 1. Then, polymers Nos. 1, 2, 3, 5, 6 and 7 were dissolved in methyl isobutyl ketone to give 15% by weight solutions, and polymers Nos. 4, 8 and 9 were dissolved in toluene to give 10% by weight solutions. Each polymer solution obtained was applied to a silicon wafer by the spin coating method to form a polymer film of about 1 pm thick.
[0048] Subsequently, the sensitivity of each polymer-applied wafer to an electron beam with an acceleration voltage of 15 kV was measured. Also, the ion etching resistance of each polymer-applied wafer was measured from the wafer's ion etching speed in ion etching under argon gas. These results are summarized in Table 1.
[0049] As is clear from Table 1, all positive type resists showed high sensitivity to the radiation and excellent dry etching resistance.
Example 4
[0050] In a sealed tube containing enclosed nitrogen gas, 8 g of phenyl isopropenyl ketone obtained in Synthesis Example 1, 5 g of methyl methacrylate and 0.1 g of azobisisobutyronitrile were statically polymerized at 60°C for 10 hours. The copolymer obtained was dissolved in 10 ml of methyl isobutyl ketone. The solution obtained was poured into 1000 ml of methanol to obtain a white precipitate.
[0051] Measurement by liquid chromatography revealed that the copolymer obtained had a weight average molecular weight of about 80,000 in terms of that of polystyrene.
[0052] Also, the copolymer was dissolved in acetone-d6 to measure NRM spectrum. The spectrum confirmed that the copolymer contained 40% by mole of phenyl isopropenyl ketone. The copolymer obtained was dissolved in methyl isobutyl ketone to give a 15% by weight solution. To this solution was added an acetone solution containing 10% by weight of trihydrate of indium nitrate so that indium nitrate became 10% by weight based on the weight of the copolymer, to give a resist solution.
[0053] This resist solution was applied to a silicon wafer at 2000 rpm by the spin coating method to form a polymer film on the wafer. Subsequently, the wafer was prebaked at 150°C for 30 min. The prebaked wafer was placed in an electron beam irradiation apparatus, wherein an electron beam with an acceleration voltage of 20 kV was applied to the wafer so as to give different dosages to different portions. Then, the irradiated wafer was taken out from the apparatus and dipped in a developer consisting of methyl isobutyl ketone and isopropyl alcohol (70 : 30 by volume) for 2 minutes for development. The developed wafer was rinsed with isopropyl alcohol to dissolve the irradiated portions. Thicknesses of the polymer film were measured by the use of a Talystep (a thin film level difference meter) at various portions exposed to different dosages.
[0054] Film thicknesses at retained portions after development (normalized) were plotted against exposure dose (coulomb/cm2) of the electron beam to give a curve of sensitivity to electron beam. From the curve, the minimum exposure dose giving zero film thickness was found to be 1.5 x 10 coulomb/cm2. Thus, the above copolymer had excellent sensitivity to the electron beam, for instance, about 50 times as high as that of poly(methyl methacrylate) and at least 5 times that of the case containing no additive.
[0055] The resist of the present invention showed good spin coating properties and excellent solvent resistance as well as good resolving power so as to resolve lines and spaces of 0.5 pm or less by the electron beam.
Example 5
[0056] In the presence of 0.1 g of azobisisobutyronitrile, 5 g of p-methylphenyl isopropenyl ketone obtained in Synthesis Example 2 and 6 g of methyl methacrylate were bulk polymerized at 40°C for 20 hours. After refining similarly to Example 1, a copolymer was obtained.
[0057] Its NMR spectrum revealed that the copolymer contained 25% by mole of p-methylphenyl isopropenyl ketone. Liquid chromatography revealed that the copolymer had a weight average molecular weight of about 70,000 in temrs of that of polystyrene. The copolymer obtained was dissolved in methyl isobutyl ketone to obtain a 15% by weight solution. To this solution were added an acetone solution containing 10% by wegiht of dihydrate of palladium chloride and an acetone solution containing 10% by weight of citraconic acid so that palladium chloride and citraconic acid became 5% by weight, respectively, based on the weight of the copolymer, to obtain a resist solution.
[0058] This resist solution was applied to a silicon wafer at 2000 rpm by the spin coating method to obtain a polymer film of 1.1 pm thick.
[0059] Subsequently, the wafer was prebaked at 150°C for 30 minutes. The prebaked wafer was kept in a sample room maintained at 10-3 Torr and soft X-rays of 8.3 R in wavelength supplied from an aluminum anticathode of rotational water cooling type with an acceleration voltage of 10 kV was applied to the wafer so as to give different dosages to different portions. The irradiated wafer was developed by dipping for 2 minutes in a developer consisting of methyl isobutyl ketone and isopropyl alcohol (70 : 30 by volume). By rinsing with isopropyl alcohol, the irradiated portions of the copolymer film were dissolved. Similarly to Example 1, retained film thicknesses after development (normalized) were plotted against exposure dose of the X-ray. From the curve thus obtained, the minimum exposure dose giving zero film thickness was found to be 10 mJ/cm2. Thus, this copolymer was highly sensitive to X-ray. Also, the copolymer showed good spin coating properties and good adhesiveness.
Example 6
[0060] Polymers of various compositions shown in Table 2 were obtained by radical polymerization at 60°C for 10 hours using as a polymerization initiator azobisisobutyronitrile. Each polymer obtained was refined similarly to Example 4 and the refined polymer was dissolved in methyl isobutyl ketone to obtain a 15% by weight solution. To this solution was added an additive in a predetermined quantity to give compositions Nos. 10 to 27 shown in Table 2. Each resulting solution was applied to a silicon wafer by the spin coating method to give a polymer film of about 1 µm thick.
[0061] Then, sensitivity of these films to an electron beam with an acceleration voltage of 20 kV was measured. Results were shown in Table 2. As is clear from Table 2, all polymers were highly sensitive to the radiation.
Comparative Example 1
[0062] Similarly to Example 1, polymers shown in Table 3 (these being outside the present invention) were obtained by radical polymerization at 80°C for 10 hours by using as a polymerization initiator azobisisobutyronitrile. Each polymer obtained was refined similarly to Examples mentioned above and the refined polymer was dissolved in toluene to give a 10% by weight solution. Each polymer solution obtained was applied to a silicon wafer by the spin coating method to give a polymer film of about 1 µm thick.
[0063] Subsequently, the sensitivity of this polymer film to an electron beam with an acceleration voltage of 15kV was measured. Also, the ion etching speed of this polymer film in the case of ion etching under argon gas was measured. These results were shown in Table 3. As is clear from Table 3, the polymers of this Comparative Example were all poor in sensitivity to the radiation and also in dry etching resistance, and hence these polymers could not be put into practical use.
Comparative Example 2
[0064] Similarly to Examples mentioned above, polymers shown in Table 4 (these being outside the present invention) were obtained by radical polymerization at 600C for 10 hours using as a polymerization initiator azobisisobutyronitrile. Each polymer obtained was refined similarly to Examples mentioned above and the refined polymer was dissolved in toluene to give a 10% by weight solution. To this solution was added an additive in a predetermined quantity to give compositions Nos. 30 to 32 shown in Table 4. Each composition was applied to a silicon wafer by the spin coating method to give a polymer film of about 1 µm thick.
1. A radiation sensitive polymer having
(a) 10 to 100% by mole of one or more repeating units of the formula:
wherein R is a hydrogen atom, a lower alkyl group, a lower alkoxy group, a halogen
atom, or a dialkylamino group, and
(b) 90 to 0% by mole of an addition polymerizable repeating unit derived from a compound
haivng CH2 = C
group in the molecule.
2. A radiation sensitive polymer according to Claim 1, wherein the addition polymerizable
repeating unit is represented by the formula:
wherein R is a lower alkyl group or a phenyl group; and R2 is -COOR3(in which R3 is a lower alkyl group or a phenyl group), -COOH, -CN, -COR4(in which R4 is a lower alkyl group), a phenyl group or a lower alkyl gorup.
wherein R is a lower alkyl group or a phenyl group; and R2 is -COOR3(in which R3 is a lower alkyl group or a phenyl group), -COOH, -CN, -COR4(in which R4 is a lower alkyl group), a phenyl group or a lower alkyl gorup.
3. A radiation sensitive polymer according to Claim 1, wherein R in the formula (1)
is a hydrogen atom, a methyl group, a methoxy group, a chlorine atom, a bromine atom,
an iodine atom, or a dimethylamino group.
4. A radiation sensitive polymer according to Claim 1, wherein the compound having
CH2 = C
group in the molecule is one member selected from the group consisting of methacrylic acid, alkyl esters of methacrylic acid, methacrylonitrile, ketones, styrene derivatives, isobutylene, and phenyl methacrylate.
group in the molecule is one member selected from the group consisting of methacrylic acid, alkyl esters of methacrylic acid, methacrylonitrile, ketones, styrene derivatives, isobutylene, and phenyl methacrylate.
5. A radiation sensitive polymer according to Claim 4, wherein the compound is methyl
methacrylate, ethyl methacrylate, propyl methacrylate, isopropyl methacrylate, butyl
methacrylate, isobutyl methacrylate, t-butyl methacrylate, cyclohexyl methacrylate,
methacrylic acid, methacrylonitrile, methyl isopropenyl ketone, a-methylstyrene, isobutylene
or phenyl methacrylate.
6. A radiation sensitive polymer according to claim 1, wherein the repeating unit
represented by the formula (1) is any one of
and the addition polymerizable repeating unit is derived from one compound selected from methacrylic acid, methyl methacrylate, methacrylonitrile and methyl isopropenyl ketone.
and the addition polymerizable repeating unit is derived from one compound selected from methacrylic acid, methyl methacrylate, methacrylonitrile and methyl isopropenyl ketone.
7. A radiation sensitive polymer material comprising
a polymer having (a) 10 to 100% by mole of one or more repeating units of the formula:
wherein R is a hydrogen atom, a lower alkyl group, a lower alkoxy group, a halogen
atom, or a dialkylamino group, and (b) 90 to 0% by mole of an addition polymerizable
repeating unit derived from a compound having
group in the molecule, in an amount of 80 to 99.9% by weight, and
(c) one compound selected from hydrates of metal chlorides and hydrates of metal nirates in an amount of 20 to 0.1% by weight.
8. A radiation sensitive polymer material according to Claim 7, wherein the addition
polymerizable repeating unit is represented by the formula:
wherein R is a lower alkyl group or a phenyl group; and R is -COOR3(in which R3 is a lower alkyl group or a phenyl group), -COOH, -CN, -COR4(in which R4 is a lower alkyl group), a phenyl group or a lower alkyl group.
wherein R is a lower alkyl group or a phenyl group; and R is -COOR3(in which R3 is a lower alkyl group or a phenyl group), -COOH, -CN, -COR4(in which R4 is a lower alkyl group), a phenyl group or a lower alkyl group.
9. A radiation sensitive polymer material according to Claim 8, wherein the compound
(c) is one member selected from the group consisting of hydrates of metal chlorides
and hydrates of metal nitrates.
10. A radiation sensitive polymer material according to Claim 7, wherein the addition
polymerizable repeating unit is derived from one compound selected from methyl methacrylate,
ethyl methacrylate, propyl methacrylate, isopropyl methacrylate, butyl methacrylate,
isobutyl methacrylate, t-butyl methacrylate, cyclohexyl methacrylate, methacrylic
acid, methacrylonitrile, methyl isopropenyl ketone, a-methylstyrene, isobutylene and
phenyl methacrylate, and the compound (c) is one member selected from the group consisting
of AlCl3·6H2O, CaCl2·6H2O, COCl2·6H2O, FeCl3·6H2O, CuCl2·2H2O, NiCl2·2H2O, PdCl2·2H2O, MnCl2·4H2O, CrCl3·6H2O, Al(NO3)3·9H2O, Zn(NO3)2·6H2O, In(NO3)3.3H2O, Ca(NO3)2· 4H2O, Cr(NO3)3·9H2O, Co(NO3)2·6H2O, Fe(NO3)3·9H2O, CU(NO3)2.3H2O, Ni(NO3)2·6H2O and Mn(NO3)2·6H2O.
11. A radiation sensitive polymer material according to Claim 7, wherein the repeating
unit represented by the formula (1) is any one of
the addition polymerizable repeating unit is derived from one compound selected from methacrylic acid, methyl methacrylate, methacrylonitrile and methyl isopropenyl ketone, and the compound (c) is one member selected from the group consisting of AlCl3.6H2O, CoCl2·6H2O, FeCl3. 6H20, CUCl2·2H2O, NiCl2·2H2O, MnCl2·4H2O, CrCl3·6H2O, Al(NO3)3·9H2O, Zn(NO3)2·5H2O,In(NO3)3·3H2O, Cr(NO3)3· 9H20, Co(NO3)2·6H2O, Fe(NO3)3·9H2O, Ni(NO3)2·6H2O and Mn(NO3)2·6H2O.
the addition polymerizable repeating unit is derived from one compound selected from methacrylic acid, methyl methacrylate, methacrylonitrile and methyl isopropenyl ketone, and the compound (c) is one member selected from the group consisting of AlCl3.6H2O, CoCl2·6H2O, FeCl3. 6H20, CUCl2·2H2O, NiCl2·2H2O, MnCl2·4H2O, CrCl3·6H2O, Al(NO3)3·9H2O, Zn(NO3)2·5H2O,In(NO3)3·3H2O, Cr(NO3)3· 9H20, Co(NO3)2·6H2O, Fe(NO3)3·9H2O, Ni(NO3)2·6H2O and Mn(NO3)2·6H2O.
12. A radiation sensitive polymer material comprising a polymer having
(a) 10 to 100% by mole of one or more repeating units represented by the formula:
wherein R is a hydrogen atom, a methyl gorup, a methoxy group, a chlorine atom,
a bromine atom, an iodine atom or a dimethylamino group, and
(b) 90 to 0% by mole of an addition polymerizable repeating unit derived from a compound
having CH2 =
group in the molecule, in an amount of 90 to 99.9% by weight, and
(c) one compound selected from hydrates of metal chlorides and hydrates of metal nitrates, in an amount of 10 to 0.1% by weight.
13. A radiation sensitive polymer material according to Claim 12, wherein the addition
polymerizable repeating unit is derived from one compound selected from methyl methacrylate,
ethyl methacrylate, propyl methacrylate, isopropyl methacrylate, butyl methacrylate,
isobutyl methacrylate, t-butyl methacrylate, cyclohexyl methacrylate, methacrylic
acid, methacrylonitrile, methyl isopropenyl ketone, a-methylstyrene, isobutylene and
phenyl methacrylate, and the compound (c) is selected from the group consisting of
AlCl3·6H2O, CaCl2·6H2O, CoCl2·6H2O,FeCl3·6H2O, CuCl2·2H2O, NiCl2·2H2O, PdCl2. 2H20, MnCl2·4H2O, CrCl3·6H2O, Al(NO3)3·9H2O, Zn(NO3)2. 6H20, In(NO3)3·3H2O, Ca(NO3)2·4H2O, Cr(NO3)3·9H2O, CO(NO3)2.6H2O, Fe(NO3)3·9H2O, "Cu(NO3)2·3H2O, Ni(NO3)2· 6H20 and Mn(NO3)2·6H2O.
14. A radiation sensitive polymer material according to Claim 12, wherein the repeating
unit represented by the formula (1) is any one of
the addition polymerizable repeating unit is derived from one compound selected from methacrylic acid, methyl methacrylate, methacrylonitrile and methyl isopropenyl ketone; and the compound (c) is selected from the group consisting-of AlCl3.6H2O CoCl2·6H2O, FeCl3·6H2O, CuCl2· 2H20, NiCl2·2H2O, MnCl2·4H2O, CrCl3·6H2O, Al(NO3)3·9H2O, Zn(NO3)2.6H2O, In(NO3)3.3H2O, Cr(NO3)·9H2O, Co(NO3)2· 6H20, Fe(NO3)3.9H2O, Ni(NO3)2·6H2O and Mn(NO3)2·6H2O.
the addition polymerizable repeating unit is derived from one compound selected from methacrylic acid, methyl methacrylate, methacrylonitrile and methyl isopropenyl ketone; and the compound (c) is selected from the group consisting-of AlCl3.6H2O CoCl2·6H2O, FeCl3·6H2O, CuCl2· 2H20, NiCl2·2H2O, MnCl2·4H2O, CrCl3·6H2O, Al(NO3)3·9H2O, Zn(NO3)2.6H2O, In(NO3)3.3H2O, Cr(NO3)·9H2O, Co(NO3)2· 6H20, Fe(NO3)3.9H2O, Ni(NO3)2·6H2O and Mn(NO3)2·6H2O.